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GII Y25T

Brand: BMC

SKU: bpap0004

₹35,000.00

• BPAP System (Y Series) is a Bi-level PAP (Bi-level Positive Airway Pressure) device, which is intended to provide non-invasive ventilation for patients with obstructive Sleep Apnea (OSA) and Respiratory Insufficiency. • It is only used for single patient and must not be re-used on another person. This is to avoid the risk of cross-infection. • The device has Ti Min/Ti Max to ensure inspiration time and improve the treatment effect significantly. It is completely Ergonomic and boasts a powerful design. • These devices are intended for adult patient by prescription in the home or hospital/institutional environment. This device is not intended for life support. • The optional Heated Humidifier used with the Y Series together is indicated for taking humidifying and heating air from the device. The optional SpO2 module used with the Y Series together is indicated for monitoring the patient's SpO2 and pulse rate auxiliarily.

Quantity

• A BIPAP is a Non invasive therapy it a pressure controlled in a spontaneous breathing. • It is used to help you breathe easier when you have condition that make breathing difficult . • Obstructive sleep apnea is a serious condition in which your breathing stop and starts repeatedly while you are asleep. • Chronic obstructive pulmonary disease (copd) • Asthma • Obesity hypoventilation syndrome. • Heart condition such as congestive heart failure or coronary artery disease • A neurological or neuromuscular disorder that affect your ability to breathe. • Poor breathing after a medical procedure such as surgery. • The machine works by pushing the pressurized air into your lungs. • It reduces burden on respiratory muscles and lungs to inhale and exhale • The machine motor blows air through the tube certain amount of required pressure. • The pressurized air enters your body through the mask or plugs. • It eliminates need for using a ventilator that makes uses of a tube that goes down into your throat without used for tracheotomy. • A tracheotomy is a procedure to create a hole in your neck to let you breathe through the trachea.

• BiPAP - Y-25T, Modes - CPAP, S, ST, T. • Type: Breathing, COPD, sleep apnea. • Usage: Ideal for COPD, Sleep apnea and obesity patient, COPD, Respiratory, Sleep apnea. • Disassembled. • Disposable. • Real-time monitoring: Tidal Volume (TV), Respiratory rate (Res Rate), Minute ventilation (Min Vent), Leakage (Leak) • Compact powerful NIV Ventilation efficacy • Volume target mode for easy synchronization of patient breathe with max pressure upto 25 cm H20

Device Size

Dimensions

 

170 mm × 180 mm × 118 mm, or 290 mm × 180 mm × 134 mm (with the humidifier)
Weight:1.5 kg, or 2.5 kg (with the humidifier)
Product Use, Transport and Storage
OperationTransport and Storage
Temperature: 5° C to 35° C (41˚F to 95˚F)-25° C to 70° C (-13˚F to 158˚F)
Humidity: 15% to 93% Non-condensing15% to 93% Non-condensing
Atmospheric Pressure: 760 ~ 1060 hPa760 ~ 1060 hPa
Mode of OperationContinuous
Work ModeCPAP, Auto, S, S/T, T
SD CardThe SD card can record patient data and fault information
AC Power Consumption100 - 240 V ~, 50 / 60 Hz, 2.0 A Max
Main Device offer to USB Communications Port5 V ~ 2.0 A
Main Device offer to Humidifier24 V ~ 1.5 A
Electric Shock
Type of Protection Against Electric ShockClass II Equipment
Degree of Protection Against Electric ShockType BF Applied Part
Degree of Protection Against Ingress of WaterIP22
Pressure Range
IPAP4.0 ~ 25.0 hPa ; in 0.5 hPa increments.
EPAP4.0 ~ 25.0 hPa ; in 0.5 hPa increments.
CPAP mode:4.0 ~ 20.0 hPa
       

Under single fault conditions,

≤ 30 hPa for CPAP mode,

≤ 40 hPa for the rest modes.

Pressure Display Accuracy± (0.8 hPa+4%)
Static Pressure Stability± 0.5 hPa
RampThe ramp time ranges from 0 to 60 minutes.
Sound Pressure Level<30 dB, when the device is working at the pressure of 10 hPa.
Sound Power Level<38 dB, when the device is working at the pressure of 10 hPa.
Maximum Flow
Test Pressure (hPa)491520
Measured Pressure at the Patient Connection Port (hPa)381419

Average Flow at the Patient

Connection Port (l/min)

75858085
SpO2 Range:

0% ~ 100%

The margin of error for SpO2 between 70% and 100% is ± 3%.

 

No strict accuracy requirements for SpO below 70%.

Pulse RateRange: 40 ~ 240 BPM
Margin of Error: ± 1%
Wavelengths

Red: 663 nanometers

Infrared: 890 nanometers

Maximal Optical Output PowerLess than 1.5 mw maximum average.
TubeLength: 6 ft. (1.83 m)
The Form and the Dimensions of the Patient Connection PortThe 22 mm conical air outlet complies with ISO 5356-1.

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